Evidence map›Paper›PMID 36750122›Full record

ArticlePhysiological reports2023

Key role for Kv11.1 (ether-a-go-go related gene) channels in rat bladder contractility.

Vincenzo Barrese, Zena Wehbe, Alice Linden, Sarah McDowell, Elizabeth Forrester, Oleksander Povstyan, Karen D McCloskey, Iain A Greenwood

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. ERG KScientific reports · 2023
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Vincenzo BarreseVascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.
Zena WehbeVascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.ORCID 0000-0003-0154-0247
Alice LindenVascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.
Sarah McDowellPatrick G. Johnston Centre for Cancer Research, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.
Elizabeth ForresterVascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.
Oleksander PovstyanInstitute of Medicine, University of Leeds, Leeds, UK.
Karen D McCloskeyPatrick G. Johnston Centre for Cancer Research, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.
Iain A GreenwoodVascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.ORCID 0000-0002-0603-0492
St George's, University of London · GBQueen's University Belfast · GBUniversity of Leeds · GB

Funding

Medical Research Council MR/M012425/1
6 · The paper itself

Abstract

In addition, to their established role in cardiac myocytes and neurons, ion channels encoded by ether-a-go-go-related genes (ERG1-3 or kcnh2,3 and 6) (kcnh2) are functionally relevant in phasic smooth muscle. The aim of the study was to determine the expression and functional impact of ERG expression products in rat urinary bladder smooth muscle using quantitative polymerase chain reaction, immunocytochemistry, whole-cell patch-clamp and isometric tension recording. kcnh2 was expressed in rat bladder, whereas kcnh6 and kcnh3 expression were negligible. Immunofluorescence for the kcnh2 expression product Kv11.1 was detected in the membrane of isolated smooth muscle cells. Potassium currents with voltage-dependent characteristics consistent with Kv11.1 channels and sensitive to the specific blocker E4031 (1 μM) were recorded from isolated detrusor smooth muscles. Disabling Kv11.1 activity with specific blockers (E4031 and dofetilide, 0.2-20 μM) augmented spontaneous contractions to a greater extent than BK

Indexed as

EtherUrinary BladderAnimalsEther-A-Go-Go Potassium ChannelsEthersEthyl EthersMembrane PotentialsMuscle, SmoothNerve Tissue ProteinsRatsEtherEther-A-Go-Go Potassium ChannelsEthersEthyl EthersKcnh3 protein, ratNerve Tissue ProteinsBK channelsdetrusor smooth muscleether-a-go-go-related geneskcnh2 geneKv11.1

Identifiers

PMID36750122
PMCPMC9904964
OpenAlexW4319335864

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.